| Literature DB >> 31615273 |
Daisuke Chinda1,2, Tadashi Shimoyama3, Tetsu Arai1, Kaori Sawada4, Kazuki Akitaya1, Sae Kudo1, Kohei Yasuda1, Kuniaki Miyazawa1, Naoki Akimoto1, Satoshi Sato1, Shiro Hayamizu1, Tetsuya Tatsuta1, Hidezumi Kikuchi1, Hiroto Hiraga1, Manabu Sawaya1, Hirotake Sakuraba1, Tatsuya Mikami5, Shigeyuki Nakaji4, Shinsaku Fukuda1.
Abstract
Endoscopic sub-mucosal dissection (ESD) is considered as a low-invasive treatment for early-stage colorectal cancer, but the degree of invasiveness has not been well investigated. The aim of this study was to evaluate the physical stress due to colorectal ESD based on changes in serum opsonic activity (SOA). SOA was examined by measuring reactive oxygen species (ROS) produced by neutrophils using lucigenin-dependent chemiluminescence (LgCL) and luminol-dependent chemiluminescence (LmCL). Sixty-nine patients were enrolled into the study and examined SOA in the morning of the day of ESD, the next day, and at four days after ESD. The peak height (PH) and area under the curve (AUC) of LgCL showed no significant difference between the day and the next day, whereas the PH and AUC for LgCL were significantly higher four days after ESD than on the day of ESD (p < .05). In contrast, the PH and AUC of LmCL showed no significant changes during the ESD perioperative period. This difference suggests that SOA changes during the colorectal ESD perioperative period involved minor increases in the production of lower-toxicity ROS. This finding supports the position that ESD is a technique that does not generate a great deal of physical stress. On the other hand, a significant increase in SOA at four days after colorectal ESD suggests that care is needed with postoperative management even after the patient has started to eat meals again.Entities:
Keywords: Chemiluminescence method; colorectal endoscopic sub-mucosal dissection; early colorectal cancer; serum opsonic activity
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Year: 2019 PMID: 31615273 DOI: 10.1080/10715762.2019.1681590
Source DB: PubMed Journal: Free Radic Res ISSN: 1029-2470